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Reduced Multidrug Susceptibility Profile Is a Common Feature of Opportunistic Fusarium Species: Fusarium Multi-Drug Resistant Pattern

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Journal J Fungi (Basel)
Date 2018 Jan 27
PMID 29371536
Citations 15
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Abstract

The resistance among various opportunistic species to different antifungal agents has emerged as a cause of public health problems worldwide. Considering the significance of multi-drug resistant (MDR), this paper emphasizes the problems associated with MDR and the need to understand its clinical significance to combat microbial infections. The search platform PubMed/MEDLINE and a review of 32 cases revealed a common multidrug-resistant profile exists, and clinically relevant members of are intrinsically resistant to most currently used antifungals. Dissemination occurs in patients with prolonged neutropenia, immune deficiency, and especially hematological malignancies. Amphotericin B displayed the lowest minimum inhibitory concentrarions (MICs) followed by voriconazole, and posaconazole. Itraconazole and fluconazole showed high MIC values, displaying in vitro resistance. Echinocandins showed the highest MIC values. Seven out of ten (70%) patients with neutropenia died, including those with fungemia that progressed to skin lesions. Clinical isolates displayed a common MDR profile and high MIC values for the most available antifungal agents with species- and strain-specific differences in antifungal susceptibility. Species identification of infections is important. While the use of natamycin resulted in a favorable outcome in keratitis, AmB and VRC are the most used agents for the treatment of fusariosis in clinical settings.

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References
1.
Bhartiya P, Daniell M, Constantinou M, Islam F, Taylor H . Fungal keratitis in Melbourne. Clin Exp Ophthalmol. 2007; 35(2):124-30. DOI: 10.1111/j.1442-9071.2006.01405.x. View

2.
Donnelley M, Zhu E, Thompson 3rd G . Isavuconazole in the treatment of invasive aspergillosis and mucormycosis infections. Infect Drug Resist. 2016; 9:79-86. PMC: 4898026. DOI: 10.2147/IDR.S81416. View

3.
Al-Hatmi A, van Diepeningen A, Curfs-Breuker I, de Hoog G, Meis J . Specific antifungal susceptibility profiles of opportunists in the Fusarium fujikuroi complex. J Antimicrob Chemother. 2014; 70(4):1068-71. DOI: 10.1093/jac/dku505. View

4.
Loeffler J, Stevens D . Antifungal drug resistance. Clin Infect Dis. 2003; 36(Suppl 1):S31-41. DOI: 10.1086/344658. View

5.
Antunes N, Hariharan S, DeAngelis L . Brain abscesses in children with cancer. Med Pediatr Oncol. 1998; 31(1):19-21. DOI: 10.1002/(sici)1096-911x(199807)31:1<19::aid-mpo4>3.0.co;2-2. View